Lucy was born completely healthy, but at 5 months old went to the ER for dehydration during what seemed like...
We’ve spent the evenings in hospitals, worrying and bracing ourselves for the worst. We’ve become students of the invisible processes in our bodies. We’ve felt the physical relief of meeting others in our situation. Their optimism, wisdom, and encouragement have carried us through.
So, we do the same for others who are now where we’ve been. We advocate in medical and pharmaceutical circles. We help doctors understand and respond to our disorder. We champion continued investment in research and therapies that improve the quality of life for every aHUS patient.
Simply put, it’s in our blood.
Your contributions fund vital research, create educational materials, and enable us to host free family conferences, where aHUS patients and caregivers can connect for the first time.
When you support the aHUS Foundation you make an impact on aHUS patients’ lives! Even a small donation now will help us advance knowledge, provide resources, and foster a sense of community among those affected by aHUS long into the future.